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Furthermore, because the experimental samples are small, the hydrocarbon expulsion path is short.
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This could be due to inhomogeneities in the samples investigated experimentally, either due to fluctuations in the N composition in the experimental samples or because of intrinsic differences between the short-range N ordering in GaNSb and in InGaNAs samples.
There were KHFGs with no corresponding transcripts in the DCM data set because these were either included in the array but with significant missing values across the experimental samples, or their probes were not included in the array.
These samples were analyzed alongside the experimental samples.
The final cultures were used to inoculate the experimental samples.
The experimental sample is φ25 × 50 mm cylindrical sample.
The experimental sample included 41 students.
Because 3 experimental samples at each timepoint were pooled (final n=2) for the PbTx study, duplicate arrays were run which included a dye swap.
Because experimental samples were collected on two separate dates, a further batch correction was applied using a parametric empirical Bayes framework [ 26].
Because of this, experimental samples were diluted to stay within a 1 6 ng/ μL range.
The poor fits cannot be attributed to very low levels of S17 in experimental samples, because the problem occurs for both the experimental N peptides from intact ribosomes and the reference N peptides.
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